MAUDE Adverse Event Report: ZIMMER BIOMET, INC. ARCOS CON SZ A STD 70MM; PROSTHESIS, HIP

Model Number	N/A
Medical Device Problem Codes	Inadequacy of Device Shape and/or Size (1583); Loosening of Implant Not Related to Bone-Ingrowth (4002)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	02/23/2022
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the patient was revised due to undersized implant, loosening, and infection approximately 3 years post implantation.Additional information on the reported event is unavailable.
Additional Manufacturer Narrative
(b)(4).Report source: (b)(6).Concomitant medical products: catalog number: 11-300914, lot number: 197870, brand name: arcos 14x190mm spl.Catalog number: 110010268, lot number:6512821, brand name: g7 osseoti multihole.Catalog number:11-301321, lot number:835680, brand name: arcos con sz a std.Catalog number:010000859, lot number: 6197089, brand name: g7 neutral e1 liner.Catalog number:650-0662, lot number:2018060606, brand name: delta ceramic fem hd.Catalog number:00223200418, lot number:64479179, brand name: cerclage cable.Catalog number:00223200418, lot number:64297449, brand name: cerclage cable.Catalog number:00223200418, lot number:64245448, brand name: cerclage cable.Multiple reports were submitted along with this report 0001825034-2022-00497, 0001825034-2022-00498.Customer has indicated that the product will not be returned to zimmer biomet for investigation.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.
Event or Problem Description
No further event information available at the time of this report.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.H6: component code: mechanical (g04) - stem.Visual examination of the provided pictures identified the head, cone body, and distal stem are all still assembled, the head appears to have some scuff marks identified as a black marking, the cone body and distal stem have bone debris still attached in some locations.Medical records/radiographs were provided and reviewed by a health care professional.A review of the available records identified no signs of loosening, wear, radiolucency, or any other contributing factors such as malalignment that would cause issues with any of the components.Implant size appears appropriate.Reported event was unable to be confirmed.A review of the device history records identified no related deviations or anomalies during manufacturing.During the investigation process a review of the sterile certifications were reviewed and found to be conforming with no applicable deviations.Devices were verified to have gone through acceptable sterilization process following iso/aami/astm & eu published guidelines.There are multiple factors that may contribute to an infection that are outside the control of zimmer biomet, such as external factors, i.E.Hospital/surgical environment, provider related risk factors, and/or patient comorbidities/risk factors.As there are no indications of a product or process issues identified affecting implant safety or effectiveness, therefore implanted products are not identified as the source or contributing to the reported infection.With the limited information about which components have the reported issues, and information obtained within the mmi report to support no problems indicated based on a single image view, a definitive root cause cannot be determined.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.

• Brand Name: ARCOS CON SZ A STD 70MM
• Common Device Name: PROSTHESIS, HIP
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 56 e. bell drive; warsaw IN 46582
• Manufacturer (Section G): ZIMMER BIOMET, INC.; 56 e. bell drive; warsaw IN 46582
• Manufacturer Contact: christina arnt ; 56 e. bell dr.; warsaw, IN 46582 ; 5745273773
• MDR Report Key: 13774594
• Report Number: 0001825034-2022-00500
• Device Sequence Number: 3906382
• Product Code: JDC
• UDI-Device Identifier: 00880304474314
• UDI-Public: (01)00880304474314((17)280702(10)835680
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K090757
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 06/15/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: 11-301321
• Device Lot Number: 835680
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/23/2022
• Supplement Date Received by Manufacturer: 06/02/2022
• Initial Report FDA Received Date: 03/15/2022
• Supplement Report FDA Received Date: 06/15/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 07/02/2018
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: N/A
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: SEE H10 NARRATIVE
• Outcome Attributed to Adverse Event: Required Intervention; Hospitalization
• Patient Age: 63 YR
• Patient Sex: Male
• Patient Weight: 89 KG